The aggregation properties of a series of deuteroporphyrin IX diesters
in the THF-Buffer (0.1 mol.L-1 Tris-HCl) aquiorgano solvent have been
studied by means of UV-Vis and fluorescence spectrometers. Experiment
al data show that the dimerization of porphyrins is mainly determined
by pi-pi interaction in pure organic solution while further aggregatio
n of porphyrins with long hydrocarbon chains is more likely driven by
hydrophobic-lipophilic interaction in aqueous-organic binary solution.
The appearance of the aggregates induces a red shift in absorption sp
ectra and fluorescence quenching in fluorescence spectra. The chain-le
ngth effect and chain-foldability effect have also been observed.